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CAS RN: 162635-04-3 | 產品號碼: T3574
產品規格
Appearance | White to Almost white powder to crystal |
Purity(HPLC)(CAD) | min. 95.0 area% |
NMR | confirm to structure |
性質
水溶性 | Insoluble |
Degree of solubility in water | 0.00005 mg/l 25 °C |
溶解性(可溶於) | Alcohol, Ethanol |
GHS
圖形表示 |
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信號詞 | Danger |
危險性說明 | H360 : May damage fertility or the unborn child. H413 : May cause long lasting harmful effects to aquatic life. |
防範說明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. P202 : Do not handle until all safety precautions have been read and understood. P201 : Obtain special instructions before use. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. P405 : Store locked up. |
相關法規
RTECS # | VE6257000 |
運輸資料
HS編碼* | 2934.99-000 |
Application
Temsirolimus: An Inhibitor of Mammalian Target of Rapamycin (mTOR)
Temsirolimus (also called CCI-779) is an inhibitor of mammalian target of rapamycin (mTOR), a serine/threonine protein kinase. Temsirolimus, the C-42 hydroxyl group ester analog of rapamycin [R0097], possesses better water solubility. Similarly to rapamycin, temsirolimus forms a complex with FK506-binding protein-12 (FKBP-12), and this complex binds and specifically acts as an allosteric inhibitor of mTOR. Inhibition of mTOR activity interferes with tumor angiogenesis,and resulted in a G1 growth arrest in treated tumor cells. (The product is for research purpose only.)
References
- Temsirolimus, an Inhibitor of Mammalian Target of Rapamycin (a review)
- Current development of mTOR inhibitors as anticancer agents (a review)
- In vitro metabolic study of temsirolimus: preparation, isolation, and identification of the metabolites
考研文獻
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